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Early-onset familial hemiplegic migraine due to a novel SCN1A mutation
INTRODUCTION: Familial hemiplegic migraine (FHM) is a rare autosomal dominant subtype of migraine with aura. The FHM3 subtype is caused by mutations in SCN1A, which is also the most frequent epilepsy gene encoding the voltage-gated Na(+) channel Na(V)1.1. The aim of this study was to explore the cli...
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| Publicat a: | Cephalalgia |
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| Autors principals: | , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
SAGE Publications
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5105328/ https://ncbi.nlm.nih.gov/pubmed/26763045 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/0333102415608360 |
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